The use of methotrexate in rheumatoid arthritis

被引:88
作者
Borchers, AT
Keen, CL
Cheema, GS
Gershwin, ME
机构
[1] Univ Calif Davis, Sch Med, Div Rheumatol Allergy & Clin Immunol, Livermore, CA 95616 USA
[2] Univ Calif Davis, Dept Nutr, Livermore, CA 95616 USA
关键词
bone marrow suppression; liver toxicity; methotrexate; rheumatoid arthritis;
D O I
10.1016/j.semarthrit.2003.12.003
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: To address the long-term efficacy and toxicity issues related to methotrexate (MTX) and compare it with other disease-modifying antirheumatic drugs (DMARDs). Methods: Review of the international literature on the clinical use of MTX in rheumatoid arthritis (RA) disease. Results: MTX has emerged as a relatively safe and effective treatment for RA that compares favorably with other therapies, particularly because of its considerably longer median drug survival. The toxicity profile of MTX is well established and includes serious and sometimes fatal liver disease, pneumonitis, and cytopenias. Hence, regular and careful monitoring of patients taking MTX is essential, particularly when MTX is combined with other DMARDs. Folate supplementation can reduce some of the most common side effects of MTX, but it has not yet been established whether this translates into a reduced risk of serious disease. Another potential approach to reducing the toxicity of MTX is therapeutic drug monitoring and dose individualization. However, correlations between pharmacokinetics and clinical response have been addressed in only a few studies and with conflicting results. Conclusions: MTX is an effective DMARD with a relatively safe profile compared with other therapies. Folate supplementation can significantly reduce the risk of MTX toxicity. Finally, it is essential that patients be monitored carefully to reduce the potential serious toxicities of MTX.
引用
收藏
页码:465 / 483
页数:19
相关论文
共 140 条
[1]  
AHERN M, 1988, J RHEUMATOL, V15, P1356
[2]  
ALARCON GS, 1992, J RHEUMATOL, V19, P1868
[3]  
Alarcon GS, 1997, ARTHRITIS RHEUM, V40, P391, DOI 10.1002/art.1780400229
[4]   Risk factors for methotrexate-induced lung injury in patients with rheumatoid arthritis - A multicenter, case-control study [J].
Alarcon, GS ;
Kremer, JM ;
Macaluso, M ;
Weinblatt, ME ;
Cannon, GW ;
Palmer, WR ;
StClair, EW ;
Sundy, JS ;
Alexander, RW ;
Smith, GJW ;
Axiotis, CA .
ANNALS OF INTERNAL MEDICINE, 1997, 127 (05) :356-+
[5]   METHOTREXATE IN RHEUMATOID-ARTHRITIS - TOXIC EFFECTS AS THE MAJOR FACTOR IN LIMITING LONG-TERM TREATMENT [J].
ALARCON, GS ;
TRACY, IC ;
BLACKBURN, WD .
ARTHRITIS AND RHEUMATISM, 1989, 32 (06) :671-676
[6]   SURVIVAL AND DRUG DISCONTINUATION ANALYSES IN A LARGE COHORT OF METHOTREXATE-TREATED RHEUMATOID-ARTHRITIS PATIENTS [J].
ALARCON, GS ;
TRACEY, IC ;
STRAND, GM ;
SINGH, K ;
MACALUSO, M .
ANNALS OF THE RHEUMATIC DISEASES, 1995, 54 (09) :708-712
[7]  
ALMAZOR MS, 2002, COCHRANE DB SYST REV, V4
[8]  
[Anonymous], 1996, Arthritis Rheum, V39, P713
[9]   Spontaneous remission of low-grade B-cell non-Hodgkin's lymphoma following withdrawal of methotrexate in a patient with rheumatoid arthritis: case report and review of the literature [J].
Baird, RD ;
van Zyl-Smit, RN ;
Dilke, T ;
Scott, SE ;
Rassam, SMB .
BRITISH JOURNAL OF HAEMATOLOGY, 2002, 118 (02) :567-568
[10]   Clinical pharmacokinetics of low-dose pulse methotrexate in rheumatoid arthritis [J].
Bannwarth, B ;
Pehourcq, F ;
Schaeverbeke, T ;
Dehais, J .
CLINICAL PHARMACOKINETICS, 1996, 30 (03) :194-210